US2012046451A1PendingUtilityA1
ANTI-lgSF4 ANTIBODY AND UTILIZATION OF THE SAME
Est. expiryFeb 28, 2025(expired)· nominal 20-yr term from priority
Inventors:Yoshikazu KurosawaYasushi AkahoriNobuhiro TakahashiAtsushi SugiokaNobuhiro HayashiAkihiko TakasakiKazuhiro SuzukiMiwa MoritaGene KurosawaSari FujiyamaSusumu TsutsumiKeiko OgawaKazuki MatsudaChiho MuramatsuYoshitaka IbaMariko SumitomoMasachika AzumaYoshinori UkaiKazuhiro Morishita
A61P 35/00A61P 31/00A61P 35/02A61P 1/16C07K 2317/622C07K 2317/52C07K 16/2803C07K 2317/565C07K 2317/732C07K 16/303A61K 2039/505C07K 2319/00C07K 2317/56G01N 33/57525G01N 33/57505
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Claims
Abstract
It is intended to clarify a molecule which is available as a target in treating or diagnosing cancer and utilize the molecule in the medical field or the research field. By treating IgSF4, which has been identified as a molecule specifically expressed in lung cancer cells, with an antibody, and ADCC activity is exerted. Based on this finding, an anti-IgSF4 antibody is provided as a means efficacious in treating cancer, etc.
Claims
exact text as granted — not AI-modified1 - 24 . (canceled)
25 . An isolated antibody having specific binding property against IgSF4, which comprises:
a heavy chain variable region having CDR containing the amino acid sequences of SEQ ID NO.: 50-52 and; a light chain variable region having CDR containing the amino acid sequences of SEQ ID NO.: 54-56.
26 . The isolated antibody according to claim 25 , which is a human antibody or a humanized antibody.
27 . The isolated antibody according to claim 25 , which is IgG, Fab, Fab′, F(ab′)2, scFv, or dsFv antibody.
28 . A therapeutic agent for cancer comprising an antibody as claimed in claim 25 as an active ingredient.
29 . A reagent comprising an antibody as claimed in claim 25 , which is used for examination of liver cancer, examination of adult T cell leukemia, study of liver cancer, or study of adult T cell leukemia.
30 . The isolated antibody according to claim 25 , which comprises:
a heavy chain variable region and a light chain variable region in a combination of a heavy chain variable region having CDR consisting of CDR1 of SEQ ID NO.:50, CDR2 of SEQ ID NO.:51, and CDR3 of SEQ ID NO.:52, and a light chain variable region having CDR consisting of CDR1 of SEQ ID NO.:54, CDR2 of SEQ ID NO.:55, and CDR3 of SEQ ID NO.:56.Join the waitlist — get patent alerts
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